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rs1060503092

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503092(A;A)
Make rs1060503092(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position133264546
GeneNDRG1
is asnp
is mentioned by
dbSNPrs1060503092
dbSNP (classic)rs1060503092
ClinGenrs1060503092
ebirs1060503092
HLIrs1060503092
Exacrs1060503092
Gnomadrs1060503092
Varsomers1060503092
LitVarrs1060503092
Maprs1060503092
PheGenIrs1060503092
Biobankrs1060503092
1000 genomesrs1060503092
hgdprs1060503092
ensemblrs1060503092
geneviewrs1060503092
scholarrs1060503092
googlers1060503092
pharmgkbrs1060503092
gwascentralrs1060503092
openSNPrs1060503092
23andMers1060503092
23andMe allrs1060503092
SNPshotrs1060503092
SNPdbers1060503092
MSV3drs1060503092
GWAS Ctlgrs1060503092
Max Magnitude0
ClinVar
Risk rs1060503092(A;A)
Alt rs1060503092(A;A)
Reference Rs1060503092(G;G)
Significance Probable-Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene NDRG1
CLNDBN Charcot-Marie-Tooth disease, type IV
Reversed 1
HGVS NC_000008.10:g.134276789C>T
CLNSRC
CLNACC RCV000468626.1,